De novo asymmetric synthesis of a 6-O-methyl-D-glycero-L- gluco-heptopyranose-derived thioglycoside for the preparation of Campylobacter jejuni NCTC11168 capsular polysaccharide fragments
Loading...
Date
Citation for Previous Publication
Link to Related Item
Abstract
Description
An enantioselective de novo synthesis of a thioglycoside derivative of the 6-O-methyl-D-glycero- L-gluco-heptopyranose residue found in the Campylobacter jejuni NCTC11168 (HS:2) capsular polysaccharide is reported. The compound is obtained from a furfural-derived chiral diol in 11 steps. Notably, compared to the only previous synthesis of this molecule, this approach significantly reduces the number of purification steps required to obtain the target.
Item Type
http://purl.org/coar/resource_type/c_6501 http://purl.org/coar/version/c_970fb48d4fbd8a85
Alternative
Other License Text / Link
Subject/Keywords
Language
en